Canonical Allele Identifier: CA242235805

Gene: SLC25A3

Linked Data

• dbSNP Id: rs1012180060
• gnomAD v3: 12-98595598-C-T
• gnomAD v4: 12-98595598-C-T
• MyVariant Identifiers: chr12:g.98989376C>T (hg19) ; chr12:g.98595598C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.98595598C>T , CM000674.2:g.98595598C>T	GRCh38
NC_000012.11:g.98989376C>T , CM000674.1:g.98989376C>T	GRCh37
NC_000012.10:g.97513507C>T	NCBI36
NG_011702.1:g.6974C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000228318.8:c.282+41C>T MANE Plus Clinical	ENSP00000228318.3:n.282+41C>T
ENST00000552981.6:c.158-129C>T MANE Select	ENSP00000448708.2:n.158-129C>T
ENST00000188376.9:c.158-129C>T	ENSP00000188376.5:n.158-129C>T
ENST00000228318.7:c.282+41C>T	ENSP00000228318.3:n.282+41C>T
ENST00000401722.7:c.158-129C>T	ENSP00000383898.3:n.158-129C>T
ENST00000546766.5:n.1710C>T
ENST00000547534.5:c.158-129C>T	ENSP00000449793.1:n.158-129C>T
ENST00000548046.5:c.282+41C>T	ENSP00000447339.1:n.282+41C>T
ENST00000548847.1:c.158-129C>T	ENSP00000449166.1:n.158-129C>T
ENST00000549338.5:c.158-129C>T	ENSP00000447740.1:n.158-129C>T
ENST00000550695.1:c.282+41C>T	ENSP00000449479.1:n.282+41C>T
ENST00000551123.5:c.*8C>T	ENSP00000449009.1:n.*8C>T
ENST00000551917.5:c.282+41C>T	ENSP00000447310.1:n.282+41C>T
ENST00000552981.5:c.158-129C>T	ENSP00000448708.1:n.158-129C>T
NM_002635.3:c.158-129C>T	NP_002626.1:n.158-129C>T
NM_005888.3:c.282+41C>T	NP_005879.1:n.282+41C>T
NM_213611.2:c.158-129C>T	NP_998776.1:n.158-129C>T
NM_002635.4:c.158-129C>T MANE Select	NP_002626.1:n.158-129C>T
NM_213611.3:c.158-129C>T	NP_998776.1:n.158-129C>T
NM_005888.4:c.282+41C>T MANE Plus Clinical	NP_005879.1:n.282+41C>T